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dc.contributor.authorYang, Yung-Hun
dc.contributor.authorJeon, Jong-Min
dc.contributor.authorKim, Jung-Ho
dc.contributor.authorSeo, Hyung-Min
dc.contributor.authorYi, Da Hye
dc.contributor.authorRha, Chokyun
dc.contributor.authorSinskey, Anthony J
dc.contributor.authorBrigham, Christopher J.
dc.date.accessioned2016-12-02T18:22:41Z
dc.date.available2016-12-02T18:22:41Z
dc.date.issued2015-05
dc.identifier.issn1226-8372
dc.identifier.issn1976-3816
dc.identifier.urihttp://hdl.handle.net/1721.1/105530
dc.description.abstractConventional solvent-based methods are still the most practical approaches for recovery of polyhydroxyalkanoate (PHA) polymer from cellular biomass, even though potential alternatives exist, including chemical, mechanical, and enzymatic methods. It is still necessary, however, to avoid dangerous and environmentally unfriendly solvents (e.g., chloroform and dichloromethane) in the polymer recovery process. In the work presented here, we applied various solvent systems to recover PHA from Ralstonia eutropha and recombinant Escherichia coli cells. It was demonstrated that methyl ethyl ketone (MEK) is a promising solvent for PHA recovery from bacterial cells, particularly for the copolymer poly(hydroxybutyrate-cohydroxyvalerate) [P(HB-co-HV)], exhibiting > 90% polymer recovery. Even though MEK did not solubilize PHAs to the same extent as chloroform, it can recover a comparable amount of polymer because of its processing advantages, such as the low viscosity of the MEK/PHA solution, and the lower density of MEK as compared to cellular components. MEK was found to be the best alternative, non-halogenated solvent among examined candidates for recovery of P(HB-co-HV) from cells. The MEK treatment of PHAcontaining cells further allowed us to eliminate several costly and lengthy steps in the extraction process, such as cell lysis, centrifugation, and filtration.en_US
dc.description.sponsorshipKorea (South). Ministry of Education (Basic Science Research Program through the National Research Foundation of Korea (NRF- 2013R1A1A2A10004690))en_US
dc.description.sponsorshipKorea Polar Research Institute (PE14030)en_US
dc.publisherThe Korean Society for Biotechnology and Bioengineeringen_US
dc.relation.isversionofhttp://dx.doi.org/10.1007/s12257-014-0546-yen_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceThe Korean Society for Biotechnology and Bioengineeringen_US
dc.titleApplication of a non-halogenated solvent, methyl ethyl ketone (MEK) for recovery of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) [P(HB-co-HV)] from bacterial cellsen_US
dc.typeArticleen_US
dc.identifier.citationYang, Yung-Hun, Jong-Min Jeon, Da Hye Yi, Jung-Ho Kim, Hyung-Min Seo, ChoKyun Rha, Anthony J. Sinskey, and Christopher J. Brigham. “Application of a Non-Halogenated Solvent, Methyl Ethyl Ketone (MEK) for Recovery of Poly(3-Hydroxybutyrate-Co-3-Hydroxyvalerate) [P(HB-Co-HV)] from Bacterial Cells.” Biotechnol Bioproc E 20, no. 2 (April 2015): 291–297.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Engineering Systems Divisionen_US
dc.contributor.mitauthorRha, Chokyun
dc.contributor.mitauthorSinskey, Anthony J
dc.contributor.mitauthorBrigham, Christopher J
dc.relation.journalBiotechnology and Bioprocess Engineeringen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2016-08-18T15:47:25Z
dc.language.rfc3066en
dc.rights.holderThe Korean Society for Biotechnology and Bioengineering and Springer-Verlag Berlin Heidelberg
dspace.orderedauthorsYang, Yung-Hun; Jeon, Jong-Min; Yi, Da Hye; Kim, Jung-Ho; Seo, Hyung-Min; Rha, ChoKyun; Sinskey, Anthony J.; Brigham, Christopher J.en_US
dspace.embargo.termsNen
dc.identifier.orcidhttps://orcid.org/0000-0002-6671-5987
dc.identifier.orcidhttps://orcid.org/0000-0002-1015-1270
mit.licenseOPEN_ACCESS_POLICYen_US


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